Isolasi dan Identifikasi Golongan Senyawa Flavonoida serta Uji Aktivitas Antibakteri dari Kulit Batang Tumbuhan Kanyere Badak (Bridelia Glauca Blume) (Phyllanthaceae)
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Date
2023Author
Lumban Toruan, Ade Theresia Ulina
Advisor(s)
Marpaung, Lamek
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Flavonoid compound from the stem bark of the Kanyere Badak plant (Bridelia glauca Blume) had been isolated. 2500 g of Kanyere Badak plant stem bark were macerated by methanol, and the methanol extract dissolved in distiled water. The distiled water solution was extracted by partitioning with ethyl acetate repeatedly until negative to 5% FeCl3. The ethyl acetate extract was dissolved in methanol and extracted by partitioning with n-hexane until the n-hexane layer was transparent. The methanol extract was analyzed by thin layer chromatography and separated by column chromatography with a stationary phase of silica gel and a mobile phase of chloroform: methanol (90:10; 80:20; 70:30; 60:40) v/v. Fractions 148-174 was purified by preparatif thin layer chromatography using benzene : asetone (80:20) v/v eluent to produce a brownish yellow paste of 10 mg at Rf value of 0,66 using chloroform:methanol (80:20) v/v as eluent. Based on the analysis of the UV-Visible spectrophotometer, it was a wavelength (λ max) of 275 nm, the FT-IR spectrum shows the presence of OH, C=C aromatic, C=O ketones, C-H, C-O-C and C-O groups. The proton Nucleus Magnetic Resonance Spectrum (1H-NMR) shows the presence of H-2’ & H-6’ protons, H-3’ & H-5’ proton and methoxy protons. Based on the data analysis and interpretation, the isolated compound was a flavonoids of the flavanones group. The antibacterial activity of total flavonoids was determined by agar disk diffusion against Staphylococcus aureus and Escherichia coli bacteria and the results showed that total flavonoids strongly inhibited the growth of Staphylococcus aureus and Escherichia coli bacteria with MIC (Minimum Inhibitory Concentration) value at a concentration of 100 mg/mL obtained a clear zone of 9.5 mm against Staphylococcus aureus bacteria and at a concentration of 100 mg/mL obtained a clear zone of 12.15 mm against Escherichia coli bacteria.
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